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- source_evidence_literature type ECO_0000212 NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_assertion description "[The skin disease erythrokeratoderma variabilis (EKV) has been shown to be associated with mutations in GJB3 and GJB4 encoding connexin (Cx)31 and Cx30.3, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_assertion evidence source_evidence_literature NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_assertion SIO_000772 16297190 NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_assertion wasDerivedFrom befree-20150227 NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_assertion wasGeneratedBy ECO_0000203 NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426621.RAd30VF7NLYY3UGRBByMm67skmg-FD4ASOh8YkH-OaTkU130_provenance.